Data / Medical devices / Israel / Surcam Medical Devices And Developments Ltd
Surcam Medical Devices And Developments Ltd: FDA-registered device maker in Nahariya Northern, Israel, 1 510(k) clearance
Surcam Medical Devices And Developments Ltd is registered with the FDA (registration 3043585140) in Nahariya Northern, Israel. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 29, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043585140
- Address
- 1 Hayotzrim, Nahariya Northern, Israel, 2231101
- Owner or operator
- Surcam Medical Devices and Developments Ltd (10095125)
- Roles
- Manufacturer
- First device listed
- January 26, 2026
- Registered through
- 2026
- Brand names listed
- Surcam Dental Implant System, Surcam Dental Implant Tools and Accessories, Surcam dental implant drills
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
| Non-Irrigation Endosseous Dental Implant Drill Bits | QRQ | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 29, 2025 | K242217 | Surcam Dental Implant System | DZE | Substantially Equivalent | Surcam Medical Devices and Developments, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Non-Irrigation Endosseous Dental Implant Drill Bits
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Implant, Endosseous, Root-Form
- All makers of Accessories, Implant, Dental, Endosseous
Updated January 29, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.